JPWO2017069195A1 - Colored adhesive tape and colored adhesive tape for fixing portable electronic device parts - Google Patents
Colored adhesive tape and colored adhesive tape for fixing portable electronic device parts Download PDFInfo
- Publication number
- JPWO2017069195A1 JPWO2017069195A1 JP2016565518A JP2016565518A JPWO2017069195A1 JP WO2017069195 A1 JPWO2017069195 A1 JP WO2017069195A1 JP 2016565518 A JP2016565518 A JP 2016565518A JP 2016565518 A JP2016565518 A JP 2016565518A JP WO2017069195 A1 JPWO2017069195 A1 JP WO2017069195A1
- Authority
- JP
- Japan
- Prior art keywords
- colored
- adhesive tape
- layer
- sensitive adhesive
- shielding layer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000002390 adhesive tape Substances 0.000 title claims abstract description 44
- 239000010410 layer Substances 0.000 claims abstract description 139
- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims abstract description 57
- 238000000034 method Methods 0.000 claims abstract description 24
- -1 polyethylene terephthalate Polymers 0.000 claims abstract description 11
- 239000012790 adhesive layer Substances 0.000 claims abstract description 9
- 229920000139 polyethylene terephthalate Polymers 0.000 claims abstract description 9
- 239000005020 polyethylene terephthalate Substances 0.000 claims abstract description 9
- 239000000463 material Substances 0.000 claims description 21
- 239000000758 substrate Substances 0.000 abstract description 12
- 239000011347 resin Substances 0.000 description 32
- 229920005989 resin Polymers 0.000 description 32
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 21
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 18
- 239000011230 binding agent Substances 0.000 description 15
- 229920006243 acrylic copolymer Polymers 0.000 description 14
- 239000000853 adhesive Substances 0.000 description 14
- 230000001070 adhesive effect Effects 0.000 description 14
- 239000000049 pigment Substances 0.000 description 14
- 239000000203 mixture Substances 0.000 description 12
- 238000005259 measurement Methods 0.000 description 11
- 239000003431 cross linking reagent Substances 0.000 description 10
- 230000009477 glass transition Effects 0.000 description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 7
- 238000011156 evaluation Methods 0.000 description 7
- 238000007639 printing Methods 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 239000000178 monomer Substances 0.000 description 6
- 238000004381 surface treatment Methods 0.000 description 6
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 5
- 239000003522 acrylic cement Substances 0.000 description 5
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 5
- 238000003851 corona treatment Methods 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 239000003505 polymerization initiator Substances 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- 238000002834 transmittance Methods 0.000 description 5
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 229920001971 elastomer Polymers 0.000 description 4
- 238000005227 gel permeation chromatography Methods 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- 229910000859 α-Fe Inorganic materials 0.000 description 4
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000007646 gravure printing Methods 0.000 description 3
- 239000012948 isocyanate Substances 0.000 description 3
- 150000002513 isocyanates Chemical class 0.000 description 3
- 239000004973 liquid crystal related substance Substances 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 229920000515 polycarbonate Polymers 0.000 description 3
- 239000004417 polycarbonate Substances 0.000 description 3
- 238000003825 pressing Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 230000005284 excitation Effects 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- 230000020169 heat generation Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 150000001451 organic peroxides Chemical class 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000003505 terpenes Chemical class 0.000 description 2
- 235000007586 terpenes Nutrition 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- FVQMJJQUGGVLEP-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOOC(C)(C)C FVQMJJQUGGVLEP-UHFFFAOYSA-N 0.000 description 1
- HCXVPNKIBYLBIT-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy 3,5,5-trimethylhexaneperoxoate Chemical compound CC(C)(C)CC(C)CC(=O)OOOC(C)(C)C HCXVPNKIBYLBIT-UHFFFAOYSA-N 0.000 description 1
- FYRCDEARNUVZRG-UHFFFAOYSA-N 1,1,5-trimethyl-3,3-bis(2-methylpentan-2-ylperoxy)cyclohexane Chemical compound CCCC(C)(C)OOC1(OOC(C)(C)CCC)CC(C)CC(C)(C)C1 FYRCDEARNUVZRG-UHFFFAOYSA-N 0.000 description 1
- KPAPHODVWOVUJL-UHFFFAOYSA-N 1-benzofuran;1h-indene Chemical compound C1=CC=C2CC=CC2=C1.C1=CC=C2OC=CC2=C1 KPAPHODVWOVUJL-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- XKBHBVFIWWDGQX-UHFFFAOYSA-N 2-bromo-3,3,4,4,5,5,5-heptafluoropent-1-ene Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(Br)=C XKBHBVFIWWDGQX-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- RTEZVHMDMFEURJ-UHFFFAOYSA-N 2-methylpentan-2-yl 2,2-dimethylpropaneperoxoate Chemical compound CCCC(C)(C)OOC(=O)C(C)(C)C RTEZVHMDMFEURJ-UHFFFAOYSA-N 0.000 description 1
- NFWPZNNZUCPLAX-UHFFFAOYSA-N 4-methoxy-3-methylaniline Chemical compound COC1=CC=C(N)C=C1C NFWPZNNZUCPLAX-UHFFFAOYSA-N 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- 239000013032 Hydrocarbon resin Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 235000011453 Vigna umbellata Nutrition 0.000 description 1
- 240000001417 Vigna umbellata Species 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- JUIBLDFFVYKUAC-UHFFFAOYSA-N [5-(2-ethylhexanoylperoxy)-2,5-dimethylhexan-2-yl] 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOC(C)(C)CCC(C)(C)OOC(=O)C(CC)CCCC JUIBLDFFVYKUAC-UHFFFAOYSA-N 0.000 description 1
- KYIKRXIYLAGAKQ-UHFFFAOYSA-N abcn Chemical compound C1CCCCC1(C#N)N=NC1(C#N)CCCCC1 KYIKRXIYLAGAKQ-UHFFFAOYSA-N 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229920006272 aromatic hydrocarbon resin Polymers 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 235000012489 doughnuts Nutrition 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 229920006332 epoxy adhesive Polymers 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000005350 fused silica glass Substances 0.000 description 1
- 125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 229920006270 hydrocarbon resin Polymers 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 238000007373 indentation Methods 0.000 description 1
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- RBQRWNWVPQDTJJ-UHFFFAOYSA-N methacryloyloxyethyl isocyanate Chemical compound CC(=C)C(=O)OCCN=C=O RBQRWNWVPQDTJJ-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000007348 radical reaction Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- OPQYOFWUFGEMRZ-UHFFFAOYSA-N tert-butyl 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOC(=O)C(C)(C)C OPQYOFWUFGEMRZ-UHFFFAOYSA-N 0.000 description 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- KEROTHRUZYBWCY-UHFFFAOYSA-N tridecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCOC(=O)C(C)=C KEROTHRUZYBWCY-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/29—Laminated material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/36—Layered products comprising a layer of synthetic resin comprising polyesters
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J201/00—Adhesives based on unspecified macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
- C09J2203/326—Applications of adhesives in processes or use of adhesives in the form of films or foils for bonding electronic components such as wafers, chips or semiconductors
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Adhesive Tapes (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
本発明は、リワーク等の際にも支持層と着色遮蔽層とが剥離してインキ剥がれが発生してしまうことがない着色粘着テープ、及び、携帯電子機器部品固定用着色粘着テープを提供することを目的とする。本発明は、ポリエチレンテレフタレートからなる支持層の少なくとも一方の表面に着色遮蔽層を有する基材と、前記基材の少なくとも前記着色遮蔽層側の表面に粘着剤層を有する着色粘着テープであって、前記着色遮蔽層は、ナノインデンテーション法により測定される23℃におけるヤング率が6.0GPa以下である着色粘着テープである。The present invention provides a colored pressure-sensitive adhesive tape in which a support layer and a colored shielding layer are peeled off even during rework and the like, and ink peeling does not occur, and a colored pressure-sensitive adhesive tape for fixing a portable electronic device component With the goal. The present invention is a substrate having a colored shielding layer on at least one surface of a support layer made of polyethylene terephthalate, and a colored adhesive tape having an adhesive layer on the surface of at least the colored shielding layer side of the substrate, The colored shielding layer is a colored adhesive tape having a Young's modulus at 23 ° C. of 6.0 GPa or less as measured by a nanoindentation method.
Description
本発明は、リワーク等の際にも支持層と着色遮蔽層とが剥離してインキ剥がれが発生してしまうことがない着色粘着テープ、及び、携帯電子機器部品固定用着色粘着テープに関する。 The present invention relates to a colored adhesive tape in which a support layer and a colored shielding layer are not peeled off even during rework or the like, and ink peeling does not occur, and a colored adhesive tape for fixing portable electronic device parts.
画像表示装置又は入力装置を搭載した携帯電子機器(例えば、携帯電話、携帯情報端末等)においては、組み立てのために粘着テープが用いられている。具体的には、バックライトユニット(BLU)と液晶ディスプレイ(LCD)を接着するために窓枠状の両面粘着テープが用いられたり、フェライトシート等の透磁率を有する磁性シートや、携帯情報端末の発熱を抑えるためのグラファイトシート等の放熱シートを携帯情報端末内部に接着したりするために両面又は片面粘着テープが用いられている。
携帯電子機器に用いられる粘着テープには、高い粘着力をはじめとする様々な性能が求められており、例えば液晶ディスプレイの視認性を向上させるために、BLUの光源であるLED光を窓枠状のテープで完全に遮蔽したり、被着体の表面を隠蔽したりする目的のためには、高い遮蔽性を有する粘着テープが求められている。In a portable electronic device (for example, a mobile phone, a portable information terminal, etc.) equipped with an image display device or an input device, an adhesive tape is used for assembly. Specifically, a window frame-shaped double-sided adhesive tape is used to bond a backlight unit (BLU) and a liquid crystal display (LCD), a magnetic sheet having magnetic permeability such as a ferrite sheet, and a portable information terminal. Double-sided or single-sided adhesive tape is used to bond a heat-dissipating sheet such as a graphite sheet for suppressing heat generation inside the portable information terminal.
Adhesive tapes used in portable electronic devices are required to have various performances including high adhesive strength. For example, in order to improve the visibility of a liquid crystal display, LED light, which is a light source of BLU, is formed into a window frame shape. For the purpose of completely shielding with this tape or concealing the surface of the adherend, an adhesive tape having high shielding properties is required.
遮蔽性に優れた粘着テープとして、例えば特許文献1には、樹脂フィルム層(支持層)と着色層(着色遮蔽層)とを有する着色基材の少なくとも一面に粘着剤層が設けられた着色粘着テープであって、該樹脂フィルム層の厚みが2〜5μm、動摩擦係数が0.1〜0.4であり、テープの総厚みが15μm以下である着色粘着テープが記載されている。 As an adhesive tape having excellent shielding properties, for example, Patent Document 1 discloses a colored adhesive in which an adhesive layer is provided on at least one surface of a colored substrate having a resin film layer (support layer) and a colored layer (colored shielding layer). A colored pressure-sensitive adhesive tape is described in which the thickness of the resin film layer is 2 to 5 μm, the dynamic friction coefficient is 0.1 to 0.4, and the total thickness of the tape is 15 μm or less.
近年、携帯電子機器をより一層薄く軽くするデザインが求められ、粘着テープもより一層薄くなってきており、総厚みが数μm〜数十μmという極めて薄い粘着テープが求められるようになってきた。しかしながら、特許文献1に記載された着色粘着テープの総厚みを薄くしようとすると、例えばリワーク等のいったん貼着した着色粘着テープを剥離する際に、支持層と着色遮蔽層とが剥離して、インキ剥がれが発生してしまうことがあるという問題があった。 In recent years, there has been a demand for designs that make portable electronic devices thinner and lighter, and adhesive tapes have become even thinner, and extremely thin adhesive tapes having a total thickness of several μm to several tens of μm have been required. However, when trying to reduce the total thickness of the colored adhesive tape described in Patent Document 1, for example, when peeling the colored adhesive tape once pasted such as rework, the support layer and the colored shielding layer are peeled off, There has been a problem that ink peeling may occur.
本発明は、上記現状に鑑み、リワーク等の際にも支持層と着色遮蔽層とが剥離してインキ剥がれが発生してしまうことがない着色粘着テープ、及び、携帯電子機器部品固定用着色粘着テープを提供することを目的とする。 In view of the above situation, the present invention provides a colored adhesive tape that does not cause peeling of the support layer and the colored shielding layer during rework and the like, and a colored adhesive for fixing portable electronic device parts. The purpose is to provide a tape.
本発明は、ポリエチレンテレフタレートからなる支持層の少なくとも一方の表面に着色遮蔽層を有する基材と、前記基材の少なくとも前記着色遮蔽層側の表面に粘着剤層を有する着色粘着テープであって、前記着色遮蔽層は、ナノインデンテーション法により測定される23℃におけるヤング率が6.0GPa以下である着色粘着テープである。
以下に本発明を詳述する。The present invention is a substrate having a colored shielding layer on at least one surface of a support layer made of polyethylene terephthalate, and a colored adhesive tape having an adhesive layer on the surface of at least the colored shielding layer side of the substrate, The colored shielding layer is a colored adhesive tape having a Young's modulus at 23 ° C. of 6.0 GPa or less as measured by a nanoindentation method.
The present invention is described in detail below.
本発明者は、従来の着色粘着テープにおいて、リワーク等の際に支持層と着色遮蔽層とが剥離してインキ剥がれが発生してしまう原因について検討した。着色粘着テープにおいては、支持層と着色遮蔽層の密着性を向上させる目的で、通常は支持層にコロナ処理等の表面処理が行われる。しかしながら、極めて薄い粘着テープが求められる用途においては、充分な粘着性を確保するために粘着剤層の厚さを一定以上にせざるを得ず、基材の厚みをできるだけ薄くせざるを得ない。このような薄い基材においては、コロナ処理等に耐えられず破れ等が発生することから、支持層に表面処理を施すことができない。このような未処理の支持層上に着色遮蔽層を積層しても、充分な密着性が得られず、リワーク等の際に支持層と着色遮蔽層とが剥離してインキ剥がれが発生してしまったものと考えられた。
これに対して本発明者は、鋭意検討の結果、着色遮蔽層のヤング率を一定以下とすることにより、表面処理が施されていない支持層上に積層した場合でも充分な密着性が発揮され、リワーク等の際にも支持層と着色遮蔽層とが剥離してインキ剥がれが発生することがない着色粘着テープが得られることを見出し、本発明を完成した。The present inventor has examined the cause of ink peeling due to peeling of the support layer and the colored shielding layer during rework or the like in the conventional colored adhesive tape. In the colored adhesive tape, the support layer is usually subjected to a surface treatment such as corona treatment for the purpose of improving the adhesion between the support layer and the colored shielding layer. However, in applications where an extremely thin adhesive tape is required, the thickness of the pressure-sensitive adhesive layer must be a certain level or more in order to ensure sufficient adhesiveness, and the thickness of the substrate must be as thin as possible. In such a thin base material, it cannot withstand corona treatment or the like, and tearing or the like occurs, so that the support layer cannot be subjected to surface treatment. Even if a colored shielding layer is laminated on such an untreated support layer, sufficient adhesion cannot be obtained, and the support layer and the colored shielding layer are peeled off during rework or the like, causing ink peeling. It was thought to have been lost.
On the other hand, as a result of intensive studies, the present inventor achieved sufficient adhesion even when laminated on a support layer not subjected to surface treatment by setting the Young's modulus of the colored shielding layer to a certain value or less. The present inventors have found that a colored pressure-sensitive adhesive tape can be obtained in which the support layer and the colored shielding layer are peeled off even during rework and the ink does not peel off.
本発明の着色粘着テープは、基材と該基材の少なくとも一方の表面に形成された粘着剤層とを有する。本発明の着色粘着テープは、一方の表面にのみ粘着剤層を有する片面粘着テープであってもよく、両面に粘着剤層を有する両面粘着テープであってもよい。 The colored pressure-sensitive adhesive tape of the present invention has a base material and a pressure-sensitive adhesive layer formed on at least one surface of the base material. The colored adhesive tape of the present invention may be a single-sided adhesive tape having an adhesive layer only on one surface, or may be a double-sided adhesive tape having an adhesive layer on both sides.
上記基材は、支持層の一方の表面に着色遮蔽層を有する多層構造からなる。上記支持層上に着色遮蔽層を形成することにより、本発明の両面粘着テープに高い遮蔽性を付与することができる。 The base material has a multilayer structure having a colored shielding layer on one surface of the support layer. By forming a colored shielding layer on the support layer, high shielding properties can be imparted to the double-sided pressure-sensitive adhesive tape of the present invention.
上記支持層は、ポリエチレンテレフタレート(PET)からなる。PETからなる支持層を用いることにより、薄くとも充分な強度と取り扱い性を有する着色粘着テープとすることができる。
上記支持層の厚みは特に限定されないが、9μm以下である場合に特に本発明が有効である。厚みが9μm以下である支持層は、コロナ処理等に耐えられず破れ等が発生しやすく、表面処理を施すことが難しい。本発明の着色粘着テープは、このような厚みが9μm以下であってコロナ処理等の表面処理を施すことができない支持層を用いた場合であっても、リワーク等の際にも支持層と着色遮蔽層とが剥離してインキ剥がれが発生してしまうことがないという優れた効果を発揮することができる。
上記支持層の厚みの下限は特に限定されないが、実質的には1μmが下限である。The support layer is made of polyethylene terephthalate (PET). By using a support layer made of PET, a colored pressure-sensitive adhesive tape having sufficient strength and handleability can be obtained even if it is thin.
The thickness of the support layer is not particularly limited, but the present invention is particularly effective when the thickness is 9 μm or less. A support layer having a thickness of 9 μm or less cannot withstand corona treatment or the like and easily breaks, and it is difficult to perform surface treatment. The colored adhesive tape of the present invention has a thickness of 9 μm or less, and even when a support layer that cannot be subjected to surface treatment such as corona treatment is used, the support layer and the support layer are colored even during reworking or the like. The excellent effect that the ink is not peeled off due to peeling from the shielding layer can be exhibited.
The lower limit of the thickness of the support layer is not particularly limited, but substantially 1 μm is the lower limit.
上記着色遮蔽層は、23℃におけるヤング率が6.0GPa以下である。上記着色遮蔽層のヤング率を調整することにより、コロナ処理等の表面処理を施されていない支持層に対しても充分な密着性を発揮して、リワーク等の際にも支持層と着色遮蔽層とが剥離してインキ剥がれが発生してしまうことがないという優れた効果を発揮することができる。これは、上記着色遮蔽層のヤング率を6.0GPa以下とすることにより、リワーク等の際に支持層と着色遮蔽層に応力がかかっても、柔軟な着色遮蔽層が伸長することにより応力を緩和するためと考えられる。上記着色遮蔽層のヤング率が5.8GPa以下であることが好ましく、5.5GPa以下であることがより好ましい。
上記着色遮蔽層のヤング率の下限は特に限定されないが、着色粘着テープの耐熱性等の観点から、1GPa以上であることが好ましい。The colored shielding layer has a Young's modulus at 23 ° C. of 6.0 GPa or less. By adjusting the Young's modulus of the colored shielding layer, sufficient adhesion is exhibited even to a support layer that has not been subjected to a surface treatment such as corona treatment, and the support layer and the colored shield are also used during rework. It is possible to exhibit an excellent effect that the layer does not peel off and ink peeling does not occur. This is because, by setting the Young's modulus of the colored shielding layer to 6.0 GPa or less, even if stress is applied to the support layer and the colored shielding layer during rework or the like, the stress is exerted by the extension of the flexible colored shielding layer. It is thought to ease. The Young's modulus of the colored shielding layer is preferably 5.8 GPa or less, and more preferably 5.5 GPa or less.
The lower limit of the Young's modulus of the colored shielding layer is not particularly limited, but is preferably 1 GPa or more from the viewpoint of the heat resistance of the colored adhesive tape.
本明細書においてヤング率は、ナノインデンテーション法により測定される23℃におけるヤング率を意味する。ナノインデンテーション法とは、超微小な荷重で圧子を測定対象に押し込み、得られた荷重−変位曲線から、測定対象の最表面微小部層の硬さや弾性率を定量する方法である。具体的には例えば、以下の方法で測定される。
即ち、着色遮蔽層を積層したポリエチレンテレフタレートフィルム(着色遮蔽フィルム)を23℃、50%RH条件下で24時間静置後、10mm×10mmの大きさに切断し、測定用の試料を作製する。なお、着色遮蔽層を積層する支持層の厚みが9μm以下の場合には、10mm×10mmの大きさに切断した着色遮蔽フィルムの非測定面に、厚み55μmの片面粘着テープ(積水化学工業株式会社製 #550M5BS)を貼付して、測定用の試料としてもよい。試料台にガラス板を固定し、ガラス板上にエポキシ系接着剤を塗布して、着色遮蔽フィルムの非着色遮蔽層側(非測定面)をガラス板上に固定する。測定装置として例えばNano Indenter XP/DCM(Keysight Technologies社製)等を用い、着色遮蔽フィルムの遮蔽層表面のヤング率を測定する。ここで、インデンターヘッドとしてXP、圧子にダイヤモンド製のバーコビッチ型を用いることができる。測定条件は、測定モードをCSM(連続剛性測定)とし、励起振動周波数を45Hz、励起振動振幅を2nm、歪速度を0.05s−1、押し込み深さを2000nm、測定点数Nを15、測定点間隔を100μm、測定温度を23℃、標準試料をフューズドシリカとすることができる。また、解析ソフトとしてのTest Works 4(Keysight Technologies社製)等を用いることができる。本明細書においては、15点測定した平均値をヤング率とする。In this specification, Young's modulus means the Young's modulus at 23 ° C. measured by the nanoindentation method. The nanoindentation method is a method of quantifying the hardness and elastic modulus of the outermost surface micro-part layer to be measured from the obtained load-displacement curve by pushing the indenter into the measurement object with a very small load. Specifically, for example, it is measured by the following method.
That is, a polyethylene terephthalate film (colored shielding film) laminated with a colored shielding layer is allowed to stand for 24 hours under conditions of 23 ° C. and 50% RH, and then cut into a size of 10 mm × 10 mm to prepare a sample for measurement. When the thickness of the support layer on which the colored shielding layer is laminated is 9 μm or less, a single-sided adhesive tape having a thickness of 55 μm (Sekisui Chemical Co., Ltd.) is applied to the non-measurement surface of the colored shielding film cut to a size of 10 mm × 10 mm. (Product # 550M5BS) may be pasted and used as a sample for measurement. A glass plate is fixed to a sample stage, an epoxy adhesive is applied on the glass plate, and the non-colored shielding layer side (non-measurement surface) of the colored shielding film is fixed on the glass plate. For example, Nano Indenter XP / DCM (manufactured by Keysight Technologies) or the like is used as a measuring device, and the Young's modulus of the shielding layer surface of the colored shielding film is measured. Here, XP can be used as an indenter head, and a Barcovic type made of diamond can be used as an indenter. The measurement conditions are CSM (continuous stiffness measurement) as the measurement mode, the excitation vibration frequency is 45 Hz, the excitation vibration amplitude is 2 nm, the strain rate is 0.05 s −1 , the indentation depth is 2000 nm, the number of measurement points N is 15, and the measurement points The interval can be 100 μm, the measurement temperature can be 23 ° C., and the standard sample can be fused silica. Also, Test Works 4 (manufactured by Keysight Technologies) as analysis software can be used. In this specification, the average value measured at 15 points is defined as the Young's modulus.
上記着色遮蔽層は特に限定されないが、印刷法により容易に上記支持層上に着色遮蔽層を形成できることから、顔料又は染料とバインダー樹脂とを含有するインキ組成物を用いてなる着色遮蔽層が好適である。 The colored shielding layer is not particularly limited, but since a colored shielding layer can be easily formed on the support layer by a printing method, a colored shielding layer using an ink composition containing a pigment or a dye and a binder resin is preferable. It is.
上記顔料又は染料としては特に限定されず、従来公知の顔料又は染料を用いることができる。上記顔料又は染料が黒色の場合には、例えば、カーボンブラック、チタンブラック等を用いることができる。上記顔料又は染料が白色の場合には、例えば、酸化チタン、炭酸カルシウム、硫酸バリウム等を用いることができる。その他の色としては、黄色酸化鉄(黄色)、べんがら(赤色)、シアニンブルー(青色)等を用いることができる。なかでも、特に高い遮蔽性を発揮できることから、カーボンブラックが好適である。 It does not specifically limit as said pigment or dye, A conventionally well-known pigment or dye can be used. When the pigment or dye is black, for example, carbon black or titanium black can be used. When the pigment or dye is white, for example, titanium oxide, calcium carbonate, barium sulfate or the like can be used. As other colors, yellow iron oxide (yellow), red bean (red), cyanine blue (blue) and the like can be used. Among these, carbon black is preferable because it can exhibit particularly high shielding properties.
上記バインダー樹脂としては特に限定されず、例えば、ポリエステル系、アクリル系、ウレタン系等のバインダー樹脂を用いることができる。なかでも、接着性に優れ、印刷も容易であることから、ポリウレタン系のバインダー樹脂が好適である。 It does not specifically limit as said binder resin, For example, binder resin, such as a polyester type, an acrylic type, a urethane type, can be used. Of these, polyurethane-based binder resins are preferred because of their excellent adhesiveness and easy printing.
上記着色遮蔽層のヤング率は、バインダー樹脂のガラス転移温度(Tg)や顔料又は染料の配合量により調整することができる。
即ち、ガラス転移温度(Tg)の低いバインダー樹脂を選択することにより、着色遮蔽層のヤング率を低くすることができる。具体的には例えば、ポリエステル系、ウレタン系及びアクリル系のバインダー樹脂においては、ガラス転移温度(Tg)が45℃以下であることを目安として、バインダー樹脂の選択を行う。なお、ここでガラス転移温度(Tg)とは、着色遮蔽層のみを示差走査熱量計で測定した値を意味する。
ヤング率を低くする観点からは、バインダー樹脂のガラス転移温度(Tg)は0℃以下であることがより好ましい。なお、ガラス転移温度(Tg)が低すぎると、溶剤に対する耐性が弱くなることがあるため、バインダー樹脂のガラス転移温度(Tg)は−20℃以上が好ましい。
また、顔料又は染料の配合量を多くすると着色遮蔽層のヤング率が高くなり、顔料又は染料の配合量を少なくすると着色遮蔽層のヤング率が低くなる。充分な遮蔽性を確保しながら上記着色遮蔽層のヤング率を調整するためには、上記バインダー樹脂と顔料又は染料との重量比率(顔料又は染料/バインダー樹脂)の好ましい下限は0.5、好ましい上限は1.5である。上記バインダー樹脂と顔料又は染料との重量比率のより好ましい下限は0.6、より好ましい上限は1.2であり、更に好ましい下限は0.8、更に好ましい上限は1.0である。The Young's modulus of the colored shielding layer can be adjusted by the glass transition temperature (Tg) of the binder resin and the blending amount of the pigment or dye.
That is, by selecting a binder resin having a low glass transition temperature (Tg), the Young's modulus of the colored shielding layer can be lowered. Specifically, for example, in a polyester-based, urethane-based, and acrylic-based binder resin, the binder resin is selected based on a glass transition temperature (Tg) of 45 ° C. or lower. Here, the glass transition temperature (Tg) means a value obtained by measuring only the colored shielding layer with a differential scanning calorimeter.
From the viewpoint of lowering the Young's modulus, the glass transition temperature (Tg) of the binder resin is more preferably 0 ° C. or lower. In addition, since the tolerance with respect to a solvent may become weak when a glass transition temperature (Tg) is too low, -20 degreeC or more is preferable for the glass transition temperature (Tg) of binder resin.
Further, when the amount of the pigment or dye is increased, the Young's modulus of the colored shielding layer is increased, and when the amount of the pigment or dye is decreased, the Young's modulus of the colored shielding layer is decreased. In order to adjust the Young's modulus of the colored shielding layer while ensuring sufficient shielding properties, the preferred lower limit of the weight ratio of the binder resin to the pigment or dye (pigment or dye / binder resin) is 0.5, preferably The upper limit is 1.5. A more preferred lower limit of the weight ratio of the binder resin and the pigment or dye is 0.6, a more preferred upper limit is 1.2, a still more preferred lower limit is 0.8, and a still more preferred upper limit is 1.0.
上記着色遮蔽層の厚みは特に限定されないが、好ましい下限は5μm、好ましい上限は8μmである。上記着色遮蔽層の厚みがこの範囲内であると、着色粘着テープの厚みを抑えながら、充分な遮蔽性を発揮することができる。上記着色遮蔽層の厚みのより好ましい下限は6μm、より好ましい上限は7μmである。 Although the thickness of the said colored shielding layer is not specifically limited, A preferable minimum is 5 micrometers and a preferable upper limit is 8 micrometers. When the thickness of the colored shielding layer is within this range, sufficient shielding properties can be exhibited while suppressing the thickness of the colored adhesive tape. The minimum with more preferable thickness of the said colored shielding layer is 6 micrometers, and a more preferable upper limit is 7 micrometers.
上記基材の厚み(上記支持層と着色遮蔽層の厚みの合計)の好ましい下限は1μm、好ましい上限は9μmである。上記基材の厚みがこの範囲内であると、総厚みが充分に薄く、高い遮蔽性と粘着性とを両立した着色粘着テープを得ることができる。上記基材の厚みのより好ましい下限は2μm、より好ましい上限は6μmである。 The preferable lower limit of the thickness of the substrate (the total thickness of the support layer and the colored shielding layer) is 1 μm, and the preferable upper limit is 9 μm. When the thickness of the base material is within this range, the total thickness is sufficiently thin, and a colored adhesive tape having both high shielding properties and adhesiveness can be obtained. The minimum with more preferable thickness of the said base material is 2 micrometers, and a more preferable upper limit is 6 micrometers.
上記支持層の一方の表面に着色遮蔽層を形成する方法としては特に限定されず、上記支持層上に上記顔料又は染料とバインダー樹脂を含有するインキ組成物を、グラビア印刷法、フレキソ印刷法、スクリーン印刷法、オフセット印刷法等の印刷方法により印刷する方法や、コンマコーター等を用いて塗工するダイレクト塗布方法等挙げられる。 The method for forming a colored shielding layer on one surface of the support layer is not particularly limited, and an ink composition containing the pigment or dye and a binder resin on the support layer, a gravure printing method, a flexographic printing method, Examples thereof include a method of printing by a printing method such as a screen printing method and an offset printing method, and a direct coating method of coating using a comma coater.
本発明の着色粘着テープは、上記基材の少なくとも上記着色遮蔽層側の表面に粘着剤層を有する。
なお、本発明の着色粘着テープにおいては、上記着色遮蔽層上に直接上記粘着剤層が配置されていてもよく、上記着色遮蔽層と上記粘着剤層との間に、例えば他の着色層や印刷層等を有してもよい。更に、上記基材の両面に着色遮蔽層を有する場合、どちらか一方の面の着色遮蔽層側の表面に粘着剤層を有してもよい。
また、本発明の着色粘着テープが両面粘着テープである場合、両面の粘着剤層は同じ組成であってもよいし、それぞれ異なる組成であってもよい。The colored pressure-sensitive adhesive tape of the present invention has a pressure-sensitive adhesive layer on at least the colored shielding layer side surface of the substrate.
In the colored pressure-sensitive adhesive tape of the present invention, the pressure-sensitive adhesive layer may be disposed directly on the colored shielding layer, and, for example, another colored layer or the like between the colored shielding layer and the pressure-sensitive adhesive layer. You may have a printing layer etc. Furthermore, when it has a colored shielding layer on both surfaces of the said base material, you may have an adhesive layer on the surface by the side of the colored shielding layer of either side.
When the colored pressure-sensitive adhesive tape of the present invention is a double-sided pressure-sensitive adhesive tape, the double-sided pressure-sensitive adhesive layers may have the same composition or different compositions.
上記粘着剤層を構成する粘着剤は特に限定されず、従来公知の粘着剤を用いることができる。なかでも、薄くとも高い粘着力を発揮できることから、アクリル系粘着剤が好ましく、ブチルアクリレート及び2−エチルヘキシルアクリレートに由来する構成単位を有するアクリル共重合体を含有するアクリル系粘着剤がより好ましい。 The adhesive which comprises the said adhesive layer is not specifically limited, A conventionally well-known adhesive can be used. Especially, since it can exhibit high adhesive force even if it is thin, an acrylic adhesive is preferable, and an acrylic adhesive containing an acrylic copolymer having a structural unit derived from butyl acrylate and 2-ethylhexyl acrylate is more preferable.
上記(メタ)アクリル共重合体中のブチルアクリレートに由来する構成単位の含有量の好ましい下限は40重量%、好ましい上限は80重量%である。上記ブチルアクリレートに由来する構成単位の含有量がこの範囲内であると、高い凝集力と粘着力、タックを発揮することができる。
上記(メタ)アクリル共重合体中の2−エチルヘキシルアクリレートに由来する構成単位の含有量の好ましい下限は10重量%、好ましい上限は50重量%である。上記2−エチルヘキシルアクリレートに由来する構成単位の含有量がこの範囲内であると、高い凝集力と優れた粘着力、タックを発揮することができる。The minimum with preferable content of the structural unit derived from the butyl acrylate in the said (meth) acrylic copolymer is 40 weight%, and a preferable upper limit is 80 weight%. When the content of the structural unit derived from the butyl acrylate is within this range, high cohesive force, adhesive force, and tack can be exhibited.
The minimum with preferable content of the structural unit derived from 2-ethylhexyl acrylate in the said (meth) acrylic copolymer is 10 weight%, and a preferable upper limit is 50 weight%. When the content of the structural unit derived from 2-ethylhexyl acrylate is within this range, high cohesive force, excellent adhesive force, and tack can be exhibited.
上記(メタ)アクリル共重合体は、必要に応じてブチルアクリレート及び2−エチルヘキシルアクリレート以外の共重合可能な他の重合性モノマーに由来する構成単位を含んでいてもよい。
上記共重合可能な他の重合性モノマーとして、例えば、(メタ)アクリル酸メチル、(メタ)アクリル酸エチル、(メタ)アクリル酸n−プロピル、(メタ)アクリル酸イソプロピル等のアルキル基の炭素数が1〜3の(メタ)アクリル酸アルキルエステル、メタクリル酸トリデシル、(メタ)アクリル酸ステアリル等のアルキル基の炭素数が13〜18の(メタ)アクリル酸アルキルエステル、(メタ)アクリル酸ヒドロキシアルキル、グリセリンジメタクリレート、(メタ)アクリル酸グリシジル、2−メタクリロイルオキシエチルイソシアネート、(メタ)アクリル酸、イタコン酸、無水マレイン酸、クロトン酸、マレイン酸、フマル酸、等の官能性モノマーが挙げられる。The (meth) acrylic copolymer may contain a structural unit derived from another copolymerizable monomer other than butyl acrylate and 2-ethylhexyl acrylate, if necessary.
Examples of other polymerizable monomers that can be copolymerized include, for example, carbon number of alkyl groups such as methyl (meth) acrylate, ethyl (meth) acrylate, n-propyl (meth) acrylate, and isopropyl (meth) acrylate. 1 to 3 (meth) acrylic acid alkyl ester, tridecyl methacrylate, and (meth) acrylic acid alkyl ester having 13 to 18 carbon atoms such as stearyl (meth) acrylate, hydroxyalkyl (meth) acrylate , Glyceryl dimethacrylate, glycidyl (meth) acrylate, 2-methacryloyloxyethyl isocyanate, (meth) acrylic acid, itaconic acid, maleic anhydride, crotonic acid, maleic acid, fumaric acid, and the like.
上記(メタ)アクリル共重合体は、上記モノマーを含有するモノマー混合物を共重合することにより調製することができる。具体的には、上記モノマー混合物を、重合開始剤の存在下にてラジカル反応させればよい。上記モノマー混合物をラジカル反応させる方法、即ち、重合方法としては、従来公知の方法が用いられ、例えば、溶液重合(沸点重合又は定温重合)、乳化重合、懸濁重合、塊状重合等が挙げられる。 The (meth) acrylic copolymer can be prepared by copolymerizing a monomer mixture containing the monomer. Specifically, the monomer mixture may be radically reacted in the presence of a polymerization initiator. As a method of radical reaction of the monomer mixture, that is, a polymerization method, a conventionally known method is used, and examples thereof include solution polymerization (boiling point polymerization or constant temperature polymerization), emulsion polymerization, suspension polymerization, bulk polymerization and the like.
上記重合開始剤は特に限定されず、例えば、有機過酸化物、アゾ化合物等が挙げられる。上記有機過酸化物として、例えば、1,1−ビス(t−ヘキシルパーオキシ)−3,3,5−トリメチルシクロヘキサン、t−ヘキシルパーオキシピバレート、t−ブチルパーオキシピバレート、2,5−ジメチル−2,5−ビス(2−エチルヘキサノイルパーオキシ)ヘキサン、t−ヘキシルパーオキシ−2−エチルヘキサノエート、t−ブチルパーオキシ−2−エチルヘキサノエート、t−ブチルパーオキシイソブチレート、t−ブチルパーオキシ−3,5,5−トリメチルヘキサノエート、t−ブチルパーオキシラウレート等が挙げられる。上記アゾ化合物として、例えば、アゾビスイソブチロニトリル、アゾビスシクロヘキサンカルボニトリル等が挙げられる。これらの重合開始剤は単独で用いてもよいし、2種以上を併用してもよい。 The said polymerization initiator is not specifically limited, For example, an organic peroxide, an azo compound, etc. are mentioned. Examples of the organic peroxide include 1,1-bis (t-hexylperoxy) -3,3,5-trimethylcyclohexane, t-hexylperoxypivalate, t-butylperoxypivalate, 2,5 -Dimethyl-2,5-bis (2-ethylhexanoylperoxy) hexane, t-hexylperoxy-2-ethylhexanoate, t-butylperoxy-2-ethylhexanoate, t-butylperoxy Examples include isobutyrate, t-butylperoxy-3,5,5-trimethylhexanoate, and t-butylperoxylaurate. Examples of the azo compound include azobisisobutyronitrile and azobiscyclohexanecarbonitrile. These polymerization initiators may be used alone or in combination of two or more.
上記(メタ)アクリル共重合体の重量平均分子量(Mw)は、好ましい下限が40万、好ましい上限が200万である。上記(メタ)アクリル共重合体の重量平均分子量がこの範囲内であると、高い凝集力と優れた粘着力、タックを発揮することができる。上記(メタ)アクリル共重合体の重量平均分子量のより好ましい下限は50万、より好ましい上限は150万である。
重量平均分子量を上記範囲に調整するためには、重合開始剤、重合温度等の重合条件を調整すればよい。
なお、重量平均分子量(Mw)とは、GPC(Gel Permeation Chromatography:ゲルパーミエーションクロマトグラフィ)による標準ポリスチレン換算の重量平均分子量である。As for the weight average molecular weight (Mw) of the said (meth) acryl copolymer, a preferable minimum is 400,000 and a preferable upper limit is 2 million. When the weight average molecular weight of the (meth) acrylic copolymer is within this range, high cohesive force, excellent adhesive force, and tack can be exhibited. The minimum with a more preferable weight average molecular weight of the said (meth) acryl copolymer is 500,000, and a more preferable upper limit is 1,500,000.
In order to adjust the weight average molecular weight within the above range, polymerization conditions such as a polymerization initiator and a polymerization temperature may be adjusted.
In addition, a weight average molecular weight (Mw) is a weight average molecular weight of standard polystyrene conversion by GPC (Gel Permeation Chromatography: gel permeation chromatography).
上記アクリル系粘着剤は、粘着付与樹脂を含有してもよい。
上記粘着付与樹脂として、例えば、ロジンエステル系樹脂、水添ロジン系樹脂、テルペン系樹脂、テルペンフェノール系樹脂、クマロンインデン系樹脂、脂環族飽和炭化水素系樹脂、C5系石油樹脂、C9系石油樹脂、C5−C9共重合系石油樹脂等が挙げられる。これらの粘着付与樹脂は単独で用いてもよいし、2種以上を併用してもよい。The acrylic pressure-sensitive adhesive may contain a tackifier resin.
Examples of the tackifier resins include rosin ester resins, hydrogenated rosin resins, terpene resins, terpene phenol resins, coumarone indene resins, alicyclic saturated hydrocarbon resins, C5 petroleum resins, and C9 resins. Examples thereof include petroleum resins and C5-C9 copolymer petroleum resins. These tackifying resins may be used alone or in combination of two or more.
上記粘着付与樹脂の含有量は特に限定されないが、上記(メタ)アクリル共重合体100重量部に対する好ましい下限は10重量部、好ましい上限は60重量部である。上記粘着付与樹脂の含有量がこの範囲内であると、上記(メタ)アクリル共重合体に優れた粘着力、タックを付与することができる。 Although content of the said tackifying resin is not specifically limited, The preferable minimum with respect to 100 weight part of said (meth) acryl copolymers is 10 weight part, and a preferable upper limit is 60 weight part. When the content of the tackifying resin is within this range, the (meth) acrylic copolymer can be provided with excellent tack and tack.
上記アクリル系粘着剤は、架橋剤が添加されることにより上記粘着剤層を構成する樹脂(上記アクリル共重合体及び/又は上記粘着付与樹脂)の主鎖間に架橋構造が形成されていることが好ましい。
上記架橋剤は特に限定されず、例えば、イソシアネート系架橋剤、アジリジン系架橋剤、エポキシ系架橋剤、金属キレート型架橋剤等が挙げられる。なかでも、イソシアネート系架橋剤が好ましい。
上記架橋剤の添加量は、上記アクリル共重合体100重量部に対して0.01〜10重量部が好ましく、0.1〜3重量部がより好ましい。In the acrylic pressure-sensitive adhesive, a cross-linking structure is formed between the main chains of the resin (the acrylic copolymer and / or the tackifying resin) constituting the pressure-sensitive adhesive layer by adding a cross-linking agent. Is preferred.
The said crosslinking agent is not specifically limited, For example, an isocyanate type crosslinking agent, an aziridine type crosslinking agent, an epoxy-type crosslinking agent, a metal chelate type crosslinking agent etc. are mentioned. Of these, isocyanate-based crosslinking agents are preferred.
The addition amount of the crosslinking agent is preferably 0.01 to 10 parts by weight and more preferably 0.1 to 3 parts by weight with respect to 100 parts by weight of the acrylic copolymer.
上記粘着剤層のゲル分率の好ましい下限は5重量%、好ましい上限は60重量%であり、より好ましい下限は10重量%、より好ましい上限は50重量%であり、更に好ましい下限は15重量%、更に好ましい上限は40重量%である。
なお、上記粘着剤層のゲル分率は、粘着剤層をW1(g)採取し、この粘着剤層を酢酸エチル中に23℃にて24時間浸漬して不溶解分を200メッシュの金網で濾過し、金網上の残渣を真空乾燥して乾燥残渣の重量W2(g)を測定し、下記式(1)により算出する。
ゲル分率(重量%)=100×W2/W1 (1)The preferred lower limit of the gel fraction of the pressure-sensitive adhesive layer is 5% by weight, the preferred upper limit is 60% by weight, the more preferred lower limit is 10% by weight, the more preferred upper limit is 50% by weight, and the still more preferred lower limit is 15% by weight. A more preferred upper limit is 40% by weight.
The gel fraction of the pressure-sensitive adhesive layer was determined by collecting W1 (g) of the pressure-sensitive adhesive layer, and immersing this pressure-sensitive adhesive layer in ethyl acetate at 23 ° C. for 24 hours, and removing the insoluble content with a 200-mesh wire mesh. The residue on the wire mesh is vacuum-dried, and the weight W2 (g) of the dry residue is measured, and calculated by the following formula (1).
Gel fraction (% by weight) = 100 × W2 / W1 (1)
上記粘着剤の厚みは特に限定されないが、好ましい下限は1μm、好ましい上限は35μmである。上記粘着剤の厚みがこの範囲内であると、総厚みが充分に薄く、高い粘着性を有する着色粘着テープを得ることができる。上記粘着剤層の厚みのより好ましい下限は2μm、より好ましい上限は20μmである。 Although the thickness of the said adhesive is not specifically limited, A preferable minimum is 1 micrometer and a preferable upper limit is 35 micrometers. When the thickness of the pressure-sensitive adhesive is within this range, a colored pressure-sensitive adhesive tape having a sufficiently thin total thickness and high adhesiveness can be obtained. The minimum with more preferable thickness of the said adhesive layer is 2 micrometers, and a more preferable upper limit is 20 micrometers.
本発明の着色粘着テープは、JIS K 7361に準ずる方法により測定した全光線透過率が3%以下であることが好ましい。全光線透過率が3%以下であることで、本発明の着色粘着テープは、近年の携帯電子機器を構成する部品を機器本体に接着固定する用途に適した、薄くかつ遮蔽性に優れたものとなる。全光線透過率が3%を超えると、例えば、フェライトシートを機器本体に接着固定するために用いたときに、フェライトシートの下地を充分に隠蔽できないことがある。全光線透過率のより好ましい上限は2.5%、更に好ましい上限は2%である。
なお、全光線透過率は、ヘーズメーター(例えば、日本電色工業社製のHaze Meter NDH4000)を用いて、23℃、湿度50%雰囲気下で測定できる。The colored adhesive tape of the present invention preferably has a total light transmittance of 3% or less as measured by a method according to JIS K 7361. Since the total light transmittance is 3% or less, the colored pressure-sensitive adhesive tape of the present invention is thin and excellent in shielding properties suitable for use in bonding and fixing components constituting recent portable electronic devices to the device main body. It becomes. When the total light transmittance exceeds 3%, for example, when the ferrite sheet is used for bonding and fixing to a device body, the base of the ferrite sheet may not be sufficiently concealed. A more preferable upper limit of the total light transmittance is 2.5%, and a further preferable upper limit is 2%.
The total light transmittance can be measured using a haze meter (for example, Haze Meter NDH4000 manufactured by Nippon Denshoku Industries Co., Ltd.) at 23 ° C. and a humidity of 50%.
本発明の着色粘着テープの製造方法として、例えば、以下のような方法が挙げられる。
まず、アクリル共重合体、粘着付与樹脂、必要に応じて架橋剤等に溶剤を加えて粘着剤Aの溶液を作製して、この粘着剤Aの溶液を、上記基材の表面に塗布し、溶液中の溶剤を完全に乾燥除去してアクリル粘着剤層Aを形成する。次に、形成されたアクリル粘着剤層Aの上に離型フィルムをその離型処理面がアクリル粘着剤層Aに対向した状態に重ね合わせる。上記積層体をゴムローラ等によって加圧することによって、基材の片面にアクリル粘着剤層を有し、かつ、アクリル粘着剤層の表面が離型フィルムで覆われた片面粘着テープを得ることができる。
また、本発明の着色粘着テープが両面粘着テープの場合には、更に、上記離型フィルムとは別の離型フィルムを用意し、この離型フィルムの離型処理面に粘着剤Bの溶液を塗布し、溶液中の溶剤を完全に乾燥除去することにより、離型フィルムの表面にアクリル粘着剤層Bが形成された積層フィルムを作製する。得られた積層フィルムをアクリル粘着剤層Aが形成された基材の裏面に、アクリル粘着剤層Bが基材の裏面に対向した状態に重ね合わせて積層体を作製する。そして、上記積層体をゴムローラ等によって加圧することによって、基材の両面にアクリル粘着剤層を有し、かつ、アクリル粘着剤層の表面が離型フィルムで覆われた両面粘着テープを得ることができる。As a manufacturing method of the colored adhesive tape of this invention, the following methods are mentioned, for example.
First, an acrylic copolymer, a tackifier resin, and if necessary, a solvent is added to a crosslinking agent or the like to prepare a solution of the adhesive A, and the adhesive A solution is applied to the surface of the substrate. The solvent in the solution is completely removed by drying to form the acrylic pressure-sensitive adhesive layer A. Next, a release film is overlaid on the formed acrylic pressure-sensitive adhesive layer A so that the release treatment surface faces the acrylic pressure-sensitive adhesive layer A. By pressing the laminate with a rubber roller or the like, a single-sided pressure-sensitive adhesive tape having an acrylic pressure-sensitive adhesive layer on one side of the substrate and the surface of the acrylic pressure-sensitive adhesive layer covered with a release film can be obtained.
When the colored pressure-sensitive adhesive tape of the present invention is a double-sided pressure-sensitive adhesive tape, a release film different from the release film is prepared, and a solution of the adhesive B is applied to the release-treated surface of the release film. The laminated film in which the acrylic pressure-sensitive adhesive layer B is formed on the surface of the release film is prepared by applying and completely removing the solvent in the solution by drying. The obtained laminated film is superposed on the back surface of the base material on which the acrylic pressure-sensitive adhesive layer A is formed, with the acrylic pressure-sensitive adhesive layer B facing the back surface of the base material to produce a laminate. Then, by pressing the laminate with a rubber roller or the like, a double-sided pressure-sensitive adhesive tape having an acrylic pressure-sensitive adhesive layer on both surfaces of the base material and having the surface of the acrylic pressure-sensitive adhesive layer covered with a release film can be obtained. it can.
また、同様の要領で積層フィルムを2組作製し、これらの積層フィルムを基材の両面のそれぞれに、積層フィルムのアクリル粘着剤層を基材に対向させた状態に重ね合わせて積層体を作製し、この積層体をゴムローラ等によって加圧することによって、基材の両面にアクリル粘着剤層を有し、かつ、アクリル粘着剤層の表面が離型フィルムで覆われた両面粘着テープを得てもよい。 In addition, two sets of laminated films are produced in the same manner, and a laminated body is produced by superposing these laminated films on both sides of the base material with the acrylic adhesive layer of the laminated film facing the base material. Then, by pressing this laminate with a rubber roller or the like, a double-sided pressure-sensitive adhesive tape having an acrylic pressure-sensitive adhesive layer on both surfaces of the base material and the surface of the acrylic pressure-sensitive adhesive layer covered with a release film can be obtained. Good.
本発明の着色粘着テープの用途は特に限定されないが、携帯電子機器を構成する部品を機器本体に接着固定する用途が好ましい。具体的には、バックライトユニット(BLU)と液晶ディスプレイ(LCD)接着固定する用途や、フェライトシート等の透磁率を有する磁性シートや携帯情報端末の発熱を抑えるためのグラファイトシート等の放熱シートを携帯情報端末内部に接着固定するために本発明の着色粘着テープを用いることができる。
本発明の着色粘着テープからなる携帯電子機器部品固定用着色粘着テープもまた、本発明の1つである。
本発明の携帯電子機器部品固定用着色粘着テープの形状は特に限定されないが、長方形、額縁状、円形、楕円形、ドーナツ型等が挙げられる。The use of the colored pressure-sensitive adhesive tape of the present invention is not particularly limited, but the use of bonding and fixing components constituting the portable electronic device to the device main body is preferable. Specifically, the adhesive unit for the backlight unit (BLU) and the liquid crystal display (LCD), a magnetic sheet having a magnetic permeability such as a ferrite sheet, and a heat radiating sheet such as a graphite sheet for suppressing heat generation of the portable information terminal. The colored pressure-sensitive adhesive tape of the present invention can be used for adhesively fixing inside a portable information terminal.
A colored adhesive tape for fixing a portable electronic device component comprising the colored adhesive tape of the present invention is also one aspect of the present invention.
The shape of the colored adhesive tape for fixing a portable electronic device component of the present invention is not particularly limited, and examples thereof include a rectangle, a frame shape, a circle, an ellipse, and a donut shape.
本発明によれば、リワーク等の際にも支持層と着色遮蔽層とが剥離してインキ剥がれが発生してしまうことがない着色粘着テープ、及び、携帯電子機器部品固定用着色粘着テープを提供することができる。 According to the present invention, there are provided a colored adhesive tape that does not cause peeling of the support layer and the colored shielding layer during rework and the like, and a colored adhesive tape for fixing portable electronic device parts. can do.
以下に実施例を挙げて本発明の態様を更に詳しく説明するが、本発明はこれら実施例にのみ限定されるものではない。 Hereinafter, embodiments of the present invention will be described in more detail with reference to examples. However, the present invention is not limited to these examples.
(実施例1)
(1)基材の調製
大日精化工業社製SKK1Cブラック−B(バインダー樹脂としてガラス転移温度(Tg)が−5.9℃であるポリエステル樹脂20.5重量部、顔料として平均粒子径が340nm、メジアン粒子径320nmのカーボンブラック12.3重量部を主成分としたインキ)100重量部に対して、硬化剤として大日精化工業社製VM−AL L8を5重量部、及び、有機溶剤として大日精化工業社製ラミックF NO.2溶剤を20重量部混合して、インキ組成物を得た。なお、SKK1Cブラック−Bに含まれる顔料の平均粒子径とメジアン粒子径は、堀場製作所社製のレーザ回折/散乱式粒子径分布測定装置LA−950を用いて測定した。
厚み6μmのポリエチレンテレフタレートフィルムからなる支持層の一方の面に、インキ組成物をグラビア印刷法により塗工、乾燥した後、40℃で36時間養生して、厚み5μmの着色遮蔽層を形成した。
得られた着色遮蔽層について、ナノインデンテーション法により23℃におけるヤング率を測定したところ、1.49GPaであった。Example 1
(1) Preparation of substrate SKK1C Black-B manufactured by Dainichi Seika Kogyo Co., Ltd. (20.5 parts by weight of a polyester resin having a glass transition temperature (Tg) of −5.9 ° C. as a binder resin, and an average particle diameter of 340 nm as a pigment) In addition, 100 parts by weight of an ink mainly composed of 12.3 parts by weight of carbon black having a median particle size of 320 nm) 5 parts by weight of VM-AL L8 manufactured by Dainichi Seika Kogyo Co., Ltd. as a curing agent, and an organic solvent Lamic F NO. 20 parts by weight of two solvents were mixed to obtain an ink composition. In addition, the average particle diameter and median particle diameter of the pigment contained in SKK1C Black-B were measured using a laser diffraction / scattering particle size distribution measuring apparatus LA-950 manufactured by Horiba.
The ink composition was applied to one surface of a support layer made of a polyethylene terephthalate film having a thickness of 6 μm, dried by gravure printing, and then cured at 40 ° C. for 36 hours to form a colored shielding layer having a thickness of 5 μm.
About the obtained colored shielding layer, it was 1.49 GPa when the Young's modulus in 23 degreeC was measured by the nanoindentation method.
(2)粘着剤の調製
温度計、攪拌機、冷却管を備えた反応器にブチルアクリレート70重量部、2−エチルヘキシルアクリレート27重量部、アクリル酸3重量部、2−ヒドロキシエチルアクリレート0.1重量部、及び、酢酸エチル80重量部を加え、窒素置換した後、反応器を加熱して還流を開始した。続いて、上記反応器内に、重合開始剤としてアゾビスイソブチロニトリル0.1重量部を添加した。70℃、5時間還流させて、アクリル共重合体の溶液を得た。得られたアクリル共重合体について、カラムとしてWater社製「2690 Separations Model」を用いてGPC法により重量平均分子量を測定したところ、71万であった。
得られたアクリル共重合体の溶液に含まれるアクリル共重合体の固形分100重量部に対して、ロジンエステル10重量(荒川化学工業社製、ペンセルD135)、テルペンフェノール10重量部(ヤスハラケミカル社製、YSポリスターT130)、酢酸エチル(不二化学薬品社製)125重量部、イソシアネート系架橋剤(日本ポリウレタン社製、コロネートL45)2重量部を添加し、攪拌して、アクリル系粘着剤を得た。(2) Preparation of pressure-sensitive adhesive A reactor equipped with a thermometer, a stirrer, and a condenser tube was 70 parts by weight of butyl acrylate, 27 parts by weight of 2-ethylhexyl acrylate, 3 parts by weight of acrylic acid, and 0.1 parts by weight of 2-hydroxyethyl acrylate. Then, 80 parts by weight of ethyl acetate was added and purged with nitrogen, and then the reactor was heated to start refluxing. Subsequently, 0.1 part by weight of azobisisobutyronitrile was added as a polymerization initiator in the reactor. The mixture was refluxed at 70 ° C. for 5 hours to obtain an acrylic copolymer solution. When the weight average molecular weight of the obtained acrylic copolymer was measured by a GPC method using “2690 Separations Model” manufactured by Water as a column, it was 710,000.
10 parts by weight of rosin ester (Arakawa Chemical Industries, Pencel D135) and 10 parts by weight of terpenephenol (manufactured by Yasuhara Chemical Co., Ltd.) with respect to 100 parts by weight of the solid content of the acrylic copolymer contained in the obtained acrylic copolymer solution. YS Polystar T130), 125 parts by weight of ethyl acetate (Fuji Chemical Co., Ltd.) and 2 parts by weight of an isocyanate-based crosslinking agent (Nihon Polyurethane Co., Coronate L45) were added and stirred to obtain an acrylic adhesive. It was.
(3)着色粘着テープの製造
厚み38μmの離型フィルム(ニッパ社製、PET38x1A3)を用意し、この離型フィルムの離型処理面に上記アクリル系粘着剤(酢酸エチルで希釈後、最終固形分20%)を塗布し、100℃で3分間乾燥させることにより、厚み10μmのアクリル系粘着剤層を形成した。このアクリル系粘着剤層を、基材の着色遮蔽層面と貼り合わせて、40℃、48時間養生して、着色粘着テープを得た。(3) Manufacture of colored adhesive tape A release film (PET38x1A3, manufactured by Nipper Co., Ltd.) having a thickness of 38 μm is prepared, and the final solid content is obtained by diluting the release film with the acrylic adhesive (ethyl acetate). 20%) was applied and dried at 100 ° C. for 3 minutes to form an acrylic pressure-sensitive adhesive layer having a thickness of 10 μm. This acrylic pressure-sensitive adhesive layer was bonded to the colored shielding layer surface of the substrate and cured at 40 ° C. for 48 hours to obtain a colored pressure-sensitive adhesive tape.
(実施例2〜11、比較例1〜4)
インキ組成物の組成を表1、2に示したようにした以外は実施例1と同様にして、着色粘着テープを得た。(Examples 2-11, Comparative Examples 1-4)
A colored adhesive tape was obtained in the same manner as in Example 1 except that the composition of the ink composition was as shown in Tables 1 and 2.
(実施例12、13)
実施例1、11と同様の方法により、厚み6μmのポリエチレンテレフタレートフィルムからなる支持層の一方の面に厚み5μmの着色遮蔽層を形成した。
白色インキ(大日精化工業社製、ラミックF 701白)を硬化剤(大日精化工業社製ラミックBハードナー)5重量部、及び、有機溶剤として大日精化工業社製ラミックF NO.2溶剤20重量部と混合して白色インキ溶液を調製した。白色インキ溶液を着色遮蔽層上にグラビア印刷法により塗工して、厚み7μmの白印刷層を形成した。
厚み38μmの離型フィルム(ニッパ社製、PET38x1A3)を用意し、この離型フィルムの離型処理面に実施例1と同様にして得られた粘着剤(酢酸エチルで希釈後、最終固形分20%)を塗布し、100℃で3分間乾燥させることにより、厚み10μmのアクリル系粘着剤層を形成した。このアクリル系粘着剤層を、基材の白色印刷層の表面と貼り合わせて、40℃、48時間養生して、着色粘着テープを得た。(Examples 12 and 13)
In the same manner as in Examples 1 and 11, a colored shielding layer having a thickness of 5 μm was formed on one surface of a support layer made of a polyethylene terephthalate film having a thickness of 6 μm.
5 parts by weight of a white ink (Dai-Nichi Seika Kogyo Co., Ltd., Lamic F 701 white) as a curing agent (Dai-Ni Seika Kogyo Co., Ltd., Lamic B Hardener) and an organic solvent, Lamic F NO. A white ink solution was prepared by mixing with 20 parts by weight of two solvents. The white ink solution was applied onto the colored shielding layer by a gravure printing method to form a white printing layer having a thickness of 7 μm.
A release film having a thickness of 38 μm (Nippa's PET38x1A3) was prepared, and the release agent surface of this release film was obtained in the same manner as in Example 1 (diluted with ethyl acetate, final solid content 20 %) And dried at 100 ° C. for 3 minutes to form an acrylic pressure-sensitive adhesive layer having a thickness of 10 μm. This acrylic pressure-sensitive adhesive layer was bonded to the surface of the white printed layer of the base material and cured at 40 ° C. for 48 hours to obtain a colored pressure-sensitive adhesive tape.
<評価>
実施例、比較例で得られた着色粘着テープについて以下の評価を行った。結果を表1、2に示した。<Evaluation>
The following evaluation was performed about the colored adhesive tape obtained by the Example and the comparative example. The results are shown in Tables 1 and 2.
(1)リワーク性の評価(対ポリカーボネート板)
得られた着色粘着テープを23℃、50%RH条件下で24時間静置後、10mm×200mmの大きさに切断して測定用テープを作製した。
測定用テープを50mm×125mm×2mm厚のポリカーボネート板に貼付し、2kgゴムローラを使用して、300mm/分・1往復で圧着を行った。圧着後すぐに85℃で24時間加熱し、その後、23℃、50%RHで3時間養生した。
その後、JIS Z 0237:2009に準ずる方法により、180°剥離試験を実施した(剥離速度は300mm/min)。剥離試験後の被着体の表面の着色物の転移(インキ剥がれ)を目視で確認し、以下の基準によりリワーク特性の官能評価を行った。
○:着色物の転移は全く認められなかった。
△:着色物の転移がわずかに確認できた。
×:着色物が全面に転移しているのが確認できた。(1) Evaluation of reworkability (vs. polycarbonate plate)
The obtained colored adhesive tape was allowed to stand at 23 ° C. and 50% RH for 24 hours, and then cut into a size of 10 mm × 200 mm to prepare a measuring tape.
A measuring tape was affixed to a polycarbonate plate having a thickness of 50 mm × 125 mm × 2 mm, and was pressure-bonded at 300 mm / min · 1 reciprocation using a 2 kg rubber roller. Immediately after the pressure bonding, it was heated at 85 ° C. for 24 hours, and then cured at 23 ° C. and 50% RH for 3 hours.
Then, the 180 degree peeling test was implemented by the method according to JISZ0237: 2009 (peeling speed is 300 mm / min). The transition (ink peeling) of the colored material on the surface of the adherend after the peeling test was visually confirmed, and sensory evaluation of rework characteristics was performed according to the following criteria.
○: No transfer of colored substances was observed.
(Triangle | delta): The transfer of the colored material was confirmed slightly.
X: It was confirmed that the colored material was transferred to the entire surface.
(2)リワーク性の評価(対ガラス板)
被着体を50mm×125mm×2mm厚のガラス板に変更した以外は、対ポリカーボネート板の場合と同様にして評価を行った。(2) Evaluation of reworkability (vs. glass plate)
Evaluation was performed in the same manner as for the polycarbonate plate except that the adherend was changed to a glass plate of 50 mm × 125 mm × 2 mm thickness.
(3)耐溶剤性の評価
酢酸エチルを充分に染み込ませた綿棒で着色遮蔽層の表面を3往復擦り、着色遮蔽層が綿棒に転移するかを確認し、以下の基準により評価を行った。
○:綿棒上に着色物の転移が全く認められなかった。
△:綿棒上に着色物の転移がわずかに確認できた。
×:着色物が全面に転移しているのが確認できた。(3) Evaluation of solvent resistance The surface of the colored shielding layer was rubbed 3 times with a cotton swab sufficiently soaked in ethyl acetate to confirm whether the colored shielding layer was transferred to the cotton swab, and evaluated according to the following criteria.
○: No transfer of coloring matter was observed on the cotton swab.
(Triangle | delta): The transfer of the colored material was slightly confirmed on the cotton swab.
X: It was confirmed that the colored material was transferred to the entire surface.
本発明によれば、リワーク等の際にも支持層と着色遮蔽層とが剥離してインキ剥がれが発生してしまうことがない着色粘着テープ、及び、携帯電子機器部品固定用着色粘着テープを提供することができる。 According to the present invention, there are provided a colored adhesive tape that does not cause peeling of the support layer and the colored shielding layer during rework and the like, and a colored adhesive tape for fixing portable electronic device parts. can do.
Claims (3)
前記着色遮蔽層は、ナノインデンテーション法により測定される23℃におけるヤング率が6.0GPa以下である
ことを特徴とする着色粘着テープ。A base material having a colored shielding layer on at least one surface of a support layer made of polyethylene terephthalate, and a colored pressure-sensitive adhesive tape having an adhesive layer on at least the colored shielding layer side surface of the base material,
The colored pressure-sensitive adhesive layer, wherein the colored shielding layer has a Young's modulus at 23 ° C. of 6.0 GPa or less as measured by a nanoindentation method.
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JP2008247960A (en) * | 2007-03-29 | 2008-10-16 | Dic Corp | Light-shielding adhesive tape and lcd module produced by using the same |
JP2010053240A (en) * | 2008-08-28 | 2010-03-11 | Dic Corp | Light-shielding adhesive tape and lcd module produced by using the same |
JP2012201733A (en) * | 2011-03-24 | 2012-10-22 | Dic Corp | Colored pressure-sensitive adhesive tape for fixing glass panel |
JP2012201734A (en) * | 2011-03-24 | 2012-10-22 | Dic Corp | Colored pressure-sensitive adhesive tape for fixing polarizing film |
JP2012201737A (en) * | 2011-03-24 | 2012-10-22 | Dic Corp | Colored pressure-sensitive adhesive tape |
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JP2012201733A (en) * | 2011-03-24 | 2012-10-22 | Dic Corp | Colored pressure-sensitive adhesive tape for fixing glass panel |
JP2012201734A (en) * | 2011-03-24 | 2012-10-22 | Dic Corp | Colored pressure-sensitive adhesive tape for fixing polarizing film |
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